Petunia-Calibrachoa Variety SAKPXC032

ABSTRACT

A petunia-calibrachoa plant designated SAKPXC032 is disclosed. Embodiments include the seeds of petunia-calibrachoa SAKPXC032, the plants of petunia-calibrachoa SAKPXC032, to plant parts of petunia-calibrachoa SAKPXC032, and methods for producing a plant produced by crossing petunia-calibrachoa SAKPXC032 with itself or with another variety. Embodiments include methods for producing a plant containing in its genetic material one or more genes or transgenes and the transgenic plants and plant parts produced by those methods. Embodiments also relate to varieties, breeding varieties, plant parts, and cells derived from petunia-calibrachoa SAKPXC032, methods for producing other lines or plant parts derived from petunia-calibrachoa SAKPXC032, and the plants, varieties, and their parts derived from use of those methods. Embodiments further include hybrid seeds, plants, and plant parts produced by crossing petunia-calibrachoa SAKPXC032 with another variety.

BACKGROUND

The embodiments recited herein relate to a novel and distinctpetunia-calibrachoa designated SAKPXC032, and to the seeds, plant parts,and tissue culture produced by that petunia-calibrachoa variety. Allpublications cited in this application are herein incorporated byreference.

Petunia and calibrachoa are closely related. In the 1990's, severalspecies of petunia were crossed with calibrachoa. The resulting hybridoffspring was named Petchoa.

The foregoing examples of the related art and limitations relatedtherewith are intended to be illustrative and not exclusive. Otherlimitations of the related art will become apparent to those of skill inthe art upon a reading of the specification.

BRIEF DESCRIPTION OF THE FIGURES

The patent or application file may contain one or more drawings executedin color and/or one or more photographs. Copies of this patent or patentapplication publication with color drawing(s) and/or photograph(s) willbe provided by the Patent Office upon request and payment of thenecessary fee.

FIG. 1 shows the overall plant habit of the plant grown in a pot.

FIG. 2 shows a close-up of the flower.

SUMMARY

The following embodiments and aspects thereof are described inconjunction with systems, tools, and methods which are meant to beexemplary, not limiting in scope.

According to one embodiment, there is provided a petunia-calibrachoaplant which is valued as breeding line enabling the development ofsuperior ornamental petunia-calibrachoa plants.

Another embodiment discloses a petunia-calibrachoa plant, wherein asample of representative sample of plant tissue of saidpetunia-calibrachoa is deposited with a Budapest Depository.

Another embodiment relates to a plant, or a part thereof, produced bygrowing petunia-calibrachoa SAKPXC032, wherein the plant part comprisesat least one cell of petunia-calibrachoa SAKPXC032.

Another embodiment relates to tissue culture produced from protoplastsor cells from the petunia-calibrachoa plants disclosed in the subjectapplication, wherein said cells or protoplasts are produced from a plantpart selected from the group consisting of pollen, ovules, embryos,protoplasts, meristematic cells, callus, pollen, leaves, ovules,anthers, cotyledons, hypocotyl, pistils, roots, root tips, flowers,seeds, petiole, and stems.

Another embodiment relates to a tissue or cell culture of regenerablecells produced from the plant of SAKPXC032 and a petunia-calibrachoaplant regenerated from the tissue or cell culture of SAKPXC032.

Another embodiment relates to a method of vegetatively propagating theplant of SAKPXC032, comprising the steps of: collecting tissue or cellscapable of being propagated from a plant of SAKPXC032; cultivating saidtissue or cells to obtain proliferated shoots; and rooting saidproliferated shoots to obtain rooted plantlets; or cultivating saidtissue or cells to obtain proliferated shoots, or to obtain plantletsand a plant produced by growing the plantlets or proliferated shoots ofsaid plant.

A further embodiment relates to a method for producing an embryo orseed, wherein the method comprises crossing a SAKPXC032 plant withanother plant and harvesting the resultant embryo or seed.

A further embodiment relates to a method for developing apetunia-calibrachoa plant in a petunia-calibrachoa plant breedingprogram, comprising applying plant breeding techniques comprisingcrossing, recurrent selection, mutation breeding, wherein said mutationbreeding selects for a mutation that is spontaneous or artificiallyinduced, backcrossing, pedigree breeding, marker enhanced selection,haploid/double haploid production, or transformation to thepetunia-calibrachoa plant of SAKPXC032, or its parts, whereinapplication of said techniques results in development of apetunia-calibrachoa plant.

A further embodiment relates to a method of introducing a mutation intothe genome of petunia-calibrachoa plant SAKPXC032, said methodcomprising mutagenesis of the plant, or plant part thereof, ofSAKPXC032, wherein said mutagenesis is selected from the groupconsisting of temperature, long-term seed storage, tissue cultureconditions, ionizing radiation, chemical mutagens, and targeting inducedlocal lesions in genomes, and wherein the resulting plant comprises atleast one genome mutation and producing plants therefrom.

A further embodiment relates to a method of editing the genome ofpetunia-calibrachoa plant SAKPXC032, wherein said method is selectedfrom the group comprising zinc finger nucleases, transcriptionactivator-like effector nucleases (TALENs), engineered homingendonucleases/meganucleases, and the clustered regularly interspacedshort palindromic repeat (CRISPR)-associated protein9 (Cas9) system, andplants produced therefrom.

A further embodiment relates to a petunia-calibrachoa seed produced bygrowing SAKPXC032.

A further embodiment relates to a method of producing apetunia-calibrachoa plant, or part thereof, by growing a seed producedon SAKPXC032.

In addition to the exemplary aspects and embodiments described above,further aspects and embodiments will become apparent by study of thefollowing descriptions.

DETAILED DESCRIPTION

Petunia-calibrachoa variety SAKPXC032 disclosed in the presentapplication has shown uniformity and stability, as described in thefollowing section via vegetative cuttings and tissue culture.Petunia-calibrachoa variety SAKPXC032 disclosed in the presentapplication has been asexually reproduced a sufficient number ofgenerations with careful attention to uniformity of plant type and hasbeen increased with continued observation for uniformity. Additionally,petunia-calibrachoa variety SAKPXC032 produces viable pollen and iscapable of being used as a parental line in breeding programs.

Origin of SAKPXC032

The present invention comprises of a new and distinct cultivar ofPetunia-Calibrachoa (Petchoa) referred to by the variety name SAKPXC032.SAKPXC032 was discovered in Kakegawa, Japan in between September toDecember 2017, and originated from a mutation of Calibrachoa-Petuniavariety SAKPXC021. SAKPXC021 has a yellow flower color and asemi-mounding plant habit. In August 2018, the plants were evaluated inMisato, Japan in an open field trial. The criteria for plant selectionincluded plant size, vibrant yellow and reddish orange flower color, andsemi-mounding plant habit. In December 2018, after the completion of thetrial, a selection was made based on the above criteria and vegetativelypropagated. In August 2019, the selection was evaluated in an open fieldin Misato, Japan. Shoot-tip cuttings of the variety were then shipped toSalinas, Calif., where the plants were regenerated and reevaluated forstability of traits. The selection subsequently was named SAKPXC032 andfound to have its unique characteristics reproduce true to type insuccessive generations of asexual propagation.

Petunia-calibrachoa variety SAKPXC032 was grown under the followingenvironmental conditions for plant growth: The terminal 1.0 to 1.5inches of an actively growing stem was excised. The vegetative cuttingswere propagated in five to six weeks. The base of the cuttings weredipped for 1 to 2 seconds in a 1:9 solution of DIP 'N GROW (1 solution:9 water), a root inducing solution, immediately prior to sticking intothe cell trays. Cuttings were stuck into plastic cell trays having 98cells, and containing a moistened peat moss-based growing medium. Forthe first week, the cuttings were misted with water from overhead for 10seconds every 30 minutes until sufficient roots were formed.

Rooted cuttings were transplanted and grown in 20 cm diameter plasticpots in a glass greenhouse located in Salinas, Calif. Pots contained apeat moss-based growing medium. Soluble fertilizer containing 20%nitrogen, 10% phosphorus and 20% potassium was applied once a day orevery other day by overhead irrigation. Pots were top-dressed with adry, slow release fertilizer containing 20% nitrogen, 10% phosphorus and18% potassium. The typical average air temperature was 24° C.

Petunia-calibrachoa variety SAKPXC032 has shown uniformity andstability, as described in the following variety descriptioninformation. Petunia-calibrachoa variety SAKPXC032 was tested foruniformity and stability a sufficient number of generations with carefulattention to uniformity of plant type and has been increased withcontinued observation for uniformity.

Petunia-calibrachoa variety SAKPXC032 has the following morphologic andother characteristics based primarily on data collected in Salinas,Calif., in September 2020. Plants were approximately 18-weeks-old fromtransplant into quart pots from rooted cuttings, pinched once duringgrowth under greenhouse conditions. Color references are to The R.H.S.Colour Chart of The Royal Horticultural Society of London (R.H.S.),6^(th) edition (2015). Anatomic labels are from The CambridgeIllustrated Glossary of Botanical Terms, by M. Hickey and C. King,Cambridge University.

TABLE 1 VARIETY DESCRIPTION INFORMATION Characteristic SAKPXC032 FormAnnual or tender perennial Habit Semi-mounding Height 19.0 cm Spread32.0 cm Time to produce a rooted cutting About 4 weeks Time to bloomfrom asexual propagation 8 to 10 weeks Stem description Dull andcircular in cross-section Number of branches 1 main stalk with 4branches and many stems Main stalk diameter 10.0 mm Branch diameter 5.0mm Stem diameter 2.5 mm Stem length 6.0 cm to 10.0 cm from attachment tobranch to inflorescence Stem color RHS144A (Strong Yellow Green) Stemanthocyanin Absent Stem internode length  5.0 mm to 15.0 mm Stempubescence and color Heavy; RHS NN155D (White) Leaf arrangementAlternate Leaf shape Elliptic Leaf apex Obtuse Leaf base Attenuate Leafmargin Entire Leaf attachment Sessile Leaf texture (both surfaces)Sticky and dull Leaf pubescence and color Moderate; RHS NN155D (White)Leaf venation Pinnate Leaf venation color, both surfaces RHS 144A(Strong Yellow Green) Leaf length 2.0 cm to 4.0 cm Leaf width 7.0 mm to2.0 cm  Leaf color Upper RHS 137A (Moderate Olive Green) Leaf ColorLower Closest to RHS 137C (Moderate Yellow Green) Leaf variegationAbsent Leaf fragrance Absent Petiole Absent Flowering habit and typeIndeterminate, solitary Total number of flowers at time of evaluationApproximately 50 Flowering requirements Will flower so long as daylength is greater than 12 hours and temperature exceeds 13° C. Number offlowers per node 1 Duration of flower life 5 days Flower shape Funnelshaped with five fused petals Flower depth 5.0 mm Flower diameter 5.0 cmto 6.0 cm Flower fragrance Absent Corolla tube length 2.5 cm Corollatube diameter at midpoint 9.0 mm Flower bud shape Cylindrical Flower budlength Approximately 3.8 cm depending on age Flower bud diameterApproximately 7.0 mm depending on age Flower bud surface texture Stickyand pubescent; RHS NN155D (White) Flower bud color RHS N144C (StrongYellow Green) on tube with RHS N144B (Strong Yellow) at tip with RHSN92A (Dark Greyish Purple) veins Peduncle length 1.75 cm to 2.0 cm Peduncle diameter 2.0 mm Peduncle pubescence and color Heavy pubescenceRHS NN15D (White) Peduncle color RHS 144B (Strong Yellow Green) Calyxdescription Composed of 5 sepals, free Sepal shape Elliptical Sepalattachment Sessile Sepal apex Obtuse Sepal base Attenuate Sepal marginEntire Sepal length 1.4 cm to 1.6 cm Sepal width 2.0 mm Sepal color(Upper & Lower) Closest to RHS 138A (Moderate Yellow Green) Petal shapeBilabiate, fused, margin cleaved Petal length One section: 2.4 cm to 2.6cm Petal width One section: 2.2 cm to 2.6 cm Petal apex Truncate Petalmargin Entire Petal texture (both surfaces) Glabrous Petal color, uppersurface Most similar to but browner than RHS 15A (Vivid Yellow) with RHS34B (Vivid Reddish Orange) near throat and edges. Younger flowers havemore RHS 42A (Vivid Reddish Orange) which fades as the flowers age.Petal color, lower surface Closest to but lighter than RHS 162A(Moderate Yellow) with midveins of RHS 145A (Strong Yellow Green) withslight RHS N77A (Greyish Purple) at edges Corolla tube color, innersurface RHS 163B (Strong Orange Yellow) at top and RHS 175A (ModerateReddish Brown) at base with some RHS N199A (Moderate Olive Brown) inveins Corolla tube color, outer surface Faded 166B (Moderate ReddishBrown) with N77A (Greyish Purple) veins and midveins of 145A (StrongYellow Green) Flower tube pubescence (Outer Tube) Heavy pubescence RHSNN15D (White) Stamen description and number 5, free, arranged adjacentto pistil, 1.6 cm in length Filament color RHS 150D (Light Yellow Green)Anther color RHS 160B (Light Yellow) Pollen color and descriptionModerate; RHS 160B (Light Yellow) Ovary description Superior Pistildescription 1 (per inflorescence); 2.1 cm in length Stigma color Closestto RHS 143A (Strong Yellow Green) Style color RHS 145C (Light YellowGreen) Fragrance Absent Fruit/seed set No seed production observed

SAKPXC032 is most similar to the commercial petunia-calibrachoa varietySAKPXC021 (U.S. Pat. No. 10,492,456), however, there are differences asdescribed in Table 2.

TABLE 2 COMPARISON WITH SIMILAR VARIETY Characteristic SAKPXC032SAKPXC021 Flower color Most similar to but browner than RHS N172D(Greyish RHS 15A (Vivid Yellow) with Orange) with closest to RHS RHS 34B(Vivid Reddish N172A (Greyish Orange) at Orange) near throat and edges.edges with Younger flowers have more RHS 172A (Strong Brown) RHS 42A(Vivid Reddish venation Orange) which fades as the flowers age Corollatube color, RHS 163B (Strong Orange RHS 200A (Dark Grayish inner surfaceYellow) at top and RHS 175A Reddish Brown) with slight (Moderate ReddishBrown) at streaking of RHS 162A base with some N199A (Moderate Yellow)(Moderate Olive Brown) in veins

SAKPXC032 differs from the parental lines as described in Table 3.

TABLE 3 COMPARISON WITH PARENTAL LINES Mutation Parent CharacteristicSAKPXC032 SAKPXC021 Flower color Yellow and Reddish Reddish Brown OrangePlant growth habit Semi-mounding Semi-mounding

Further Embodiments

Breeding with Petunia-Calibrachoa Variety SAKPXC032

The complexity of inheritance influences choice of the breeding method.Backcross breeding is used to transfer one or a few favorable genes fora highly heritable trait into a desirable variety. This approach hasbeen used extensively for breeding disease-resistant varieties. Variousrecurrent selection techniques are used to improve quantitativelyinherited traits controlled by numerous genes. The use of recurrentselection in self-pollinating crops depends on the ease of pollination,the frequency of successful hybrids from each pollination, and thenumber of hybrid offspring from each successful cross.

Promising advanced breeding varieties are thoroughly tested and comparedto appropriate standards in environments representative of thecommercial target area(s) for three or more years. The best varietiesare candidates for new commercial varieties; those still deficient in afew traits may be used as parents to produce new populations for furtherselection.

These processes, which lead to the final step of marketing anddistribution, are time-consuming and require precise forward planning,efficient use of resources, and a minimum of changes in direction.

A most difficult task is the identification of individuals that aregenetically superior, because for most traits the true genotypic valueis masked by other confounding plant traits or environmental factors.One method of identifying a superior plant is to observe its performancerelative to other experimental plants and to a widely grown standardvariety. If a single observation is inconclusive, replicatedobservations provide a better estimate of its genetic worth.

The goal of petunia-calibrachoa breeding is to develop new and superiorpetunia-calibrachoa varieties and hybrids. The breeder initially selectsand crosses two or more parental varieties, followed by repeated selfingand selection, producing many new genetic combinations. The breeder cantheoretically generate billions of different genetic combinations viacrossing, selection, selfing, and mutations.

Using Petunia-Calibrachoa Variety SAKPXC032 to Develop OtherPetunia-Calibrachoa Varieties

Petunia-calibrachoa varieties such as petunia-calibrachoa varietySAKPXC032 are a source of breeding material that may be used to developnew petunia-calibrachoa varieties. Plant breeding techniques known inthe art and used in a petunia-calibrachoa breeding program include, butare not limited to, recurrent selection, mass selection, bulk selection,mass selection, backcrossing, pedigree breeding, open pollinationbreeding, restriction fragment length polymorphism enhanced selection,genetic marker enhanced selection, making double haploids,transformation, and gene editing. These techniques can be usedsingularly or in combinations. There are many analytical methodsavailable to evaluate a new variety. The oldest and most traditionalmethod of analysis is the observation of phenotypic traits, butgenotypic analysis may also be used.

Additional Breeding Methods

Any plants produced using the SAKPXC032 plants disclosed in the presentapplication as at least one parent are also an embodiment. These methodsare well-known in the art and some of the more commonly used breedingmethods are described herein. Descriptions of breeding methods can befound in one of several reference books (e.g., Allard, “Principles ofPlant Breeding” (1999); and Vainstein, “Breeding for Ornamentals:Classical and Molecular Approaches,” Kluwer Academic Publishers (2002);Callaway, “Breeding Ornamental Plants,” Timber Press (2000).

Breeding steps that may be used in the petunia-calibrachoa varietySAKPXC032 plant breeding program can include for example, pedigreebreeding, backcrossing, mutation breeding, and recurrent selection. Inconjunction with these steps, techniques such as RFLP-enhancedselection, genetic marker enhanced selection (for example, SSR markers),Gene Editing and the making of double haploids may be utilized.

As used herein, the term “plant” or plant part includes plant cells,plant protoplasts, plant cell tissue cultures from which SAKPXC032plants can be regenerated, plant calli, plant clumps, and plant cellsthat are intact in plants or parts of plants, such as pollen, ovules,embryos, protoplasts, meristematic cells, callus, pollen, leaves,ovules, anthers, cotyledons, hypocotyl, pistils, roots, root tips,seeds, flowers, petiole, pods, shoot, or stems and the like.

Pedigree Breeding

Pedigree breeding starts with the crossing of two genotypes, such aspetunia-calibrachoa variety SAKPXC032 and another petunia-calibrachoavariety having one or more desirable characteristics that is lacking orwhich complements petunia-calibrachoa variety SAKPXC032. If the twooriginal parents do not provide all the desired characteristics, othersources can be included in the breeding population. In the pedigreemethod, superior plants are selfed and selected in successive filialgenerations. In the succeeding filial generations, the heterozygouscondition gives way to homogeneous varieties as a result ofself-pollination and selection. Typically, in the pedigree method ofbreeding, five or more successive filial generations of selfing andselection is practiced: F₁ to F₂; F₂ to F₃; F₃ to F₄; F₄ to F₅; etc.After a sufficient amount of inbreeding, successive filial generationswill serve to increase seed of the developed variety. Preferably, thedeveloped variety comprises homozygous alleles at about 95% or more ofits loci.

Backcross Breeding

Backcross breeding has been used to transfer genes for a simplyinherited, highly heritable trait into a desirable homozygous variety orinbred variety which is the recurrent parent. The source of the trait tobe transferred is called the donor parent. After the initial cross,individuals possessing the phenotype of the donor parent are selectedand repeatedly crossed (backcrossed) to the recurrent parent. Theresulting plant is expected to have the attributes of the recurrentparent (e.g., variety) and the desirable trait transferred from thedonor parent. This is also known as single gene conversion and/orbackcross conversion.

In addition to being used to create a backcross conversion, backcrossingcan also be used in combination with pedigree breeding. As discussedpreviously, backcrossing can be used to transfer one or morespecifically desirable traits from one variety, the donor parent, to adeveloped variety called the recurrent parent, which has overall goodcommercial characteristics yet lacks that desirable trait or traits.However, the same procedure can be used to move the progeny toward thegenotype of the recurrent parent, but at the same time retain manycomponents of the nonrecurrent parent by stopping the backcrossing at anearly stage and proceeding with selfing and selection. As used herein,progeny refers to the descendants of one or more of the parental linesand includes an F₁ petunia-calibrachoa plant produced from the cross oftwo petunia-calibrachoa plants where at least one plant includes apetunia-calibrachoa plant disclosed herein and progeny further includes,but is not limited to, subsequent F₂, F₃, F₄, F₅, F₆, F₇, F₈, F₉, andF₁₀ generational crosses with the recurrent parental line. For example,a petunia-calibrachoa plant may be crossed with another variety toproduce a first-generation progeny plant. The first-generation progenyplant may then be backcrossed to one of its parent varieties to create aBC₁ or BC₂. Progeny are selfed and selected so that the newly developedvariety has many of the attributes of the recurrent parent and yetseveral of the desired attributes of the nonrecurrent parent. Thisapproach leverages the value and strengths of the recurrent parent foruse in new petunia-calibrachoa varieties.

Therefore, another embodiment is a method of making a backcrossconversion of petunia-calibrachoa variety SAKPXC032, comprising thesteps of crossing petunia-calibrachoa variety SAKPXC032 with a donorplant comprising a desired trait, selecting an F₁ progeny plantcomprising the desired trait, and backcrossing the selected F₁ progenyplant to petunia-calibrachoa variety SAKPXC032. This method may furthercomprise the step of obtaining a molecular marker profile ofpetunia-calibrachoa variety SAKPXC032 and using the molecular markerprofile to select for a progeny plant with the desired trait and themolecular marker profile of petunia-calibrachoa variety SAKPXC032.

Recurrent Selection and Mass Selection

Recurrent selection is a method used in a plant breeding program toimprove a population of plants. Petunia-calibrachoa variety SAKPXC032 issuitable for use in a recurrent selection program. The method entailsindividual plants cross pollinating with each other to form progeny. Theprogeny are grown and the superior progeny selected by any number ofselection methods, which include individual plant, half-sib progeny,full-sib progeny, and selfed progeny. The selected progeny are crosspollinated with each other to form progeny for another population. Thispopulation is planted and again superior plants are selected to crosspollinate with each other. Recurrent selection is a cyclical process andtherefore can be repeated as many times as desired. The objective ofrecurrent selection is to improve the traits of a population. Theimproved population can then be used as a source of breeding material toobtain new varieties for commercial or breeding use, including theproduction of a synthetic variety. A synthetic variety is the resultantprogeny formed by the intercrossing of several selected varieties.

Mass selection is a useful technique when used in conjunction withmolecular marker enhanced selection. In mass selection, seeds fromindividuals are selected based on phenotype or genotype. These selectedseeds are then bulked and used to grow the next generation. Bulkselection requires growing a population of plants in a bulk plot,allowing the plants to self-pollinate, harvesting the seed in bulk, andthen using a sample of the seed harvested in bulk to plant the nextgeneration. Also, instead of self-pollination, directed pollinationcould be used as part of the breeding program.

Mass and recurrent selections can be used to improve populations ofeither self- or cross-pollinating crops. A genetically variablepopulation of heterozygous individuals is either identified, or created,by intercrossing several different parents. The plants are selectedbased on individual superiority, outstanding progeny, or excellentcombining ability. The selected plants are intercrossed to produce a newpopulation in which further cycles of selection are continued.

Protoplast Fusion

Also known as somatic fusion, this process can be used with SAKPXC032 tocreate hybrids. The resulting hybrid plants have the chromosomes of eachparent and thus the process is useful for incorporating new traits. Theprotoplast fusion technique is well known in the art; see for exampleHamill J. D., Cocking E. C. (1988) Somatic Hybridization of Plants andits Use in Agriculture. In: Pais M. S. S., Mavituna F., Novais J. M.(eds) Plant Cell Biotechnology. NATO ASI Series (Series H: CellBiology), vol 18.

Mutation Breeding

Mutation breeding is another method of introducing new traits intopetunia-calibrachoa variety SAKPXC032. Mutations that occurspontaneously or are artificially induced can be useful sources ofvariability for a plant breeder. The goal of artificial mutagenesis isto increase the rate of mutation for a desired characteristic. Mutationrates can be increased by many different means including temperature,long-term seed storage, tissue culture conditions, ionizing radiation,such as X-rays, Gamma rays (e.g., cobalt 60 or cesium 137), neutrons,(product of nuclear fission by uranium 235 in an atomic reactor), Betaradiation (emitted from radioisotopes such as phosphorus 32 or carbon14), or ultraviolet radiation (preferably from 2500 to 2900 nm);chemical mutagens (such as base analogues (5-bromo-uracil)), relatedcompounds (8-ethoxy caffeine), antibiotics (streptonigrin), alkylatingagents (sulfur mustards, nitrogen mustards, epoxides, ethylenamines,sulfates, sulfonates such as ethyl methanesulfonate, sulfones,lactones), sodium azide, hydroxylamine, nitrous acid,methylnitrilsourea, or acridines; TILLING (targeting induced locallesions in genomes), where mutation is induced by chemical mutagens andmutagenesis is accompanied by the isolation of chromosomal DNA fromevery mutated plant line or seed and screening of the population of theseed or plants is performed at the DNA level using advanced moleculartechniques. Once a desired trait is observed through mutagenesis thetrait may then be incorporated into existing germplasm by traditionalbreeding techniques. Details of mutation breeding can be found inVainstein, “Breeding for Ornamentals: Classical and MolecularApproaches,” Kluwer Academic Publishers (2002); Sikora, Per, et al.,“Mutagenesis as a Tool in Plant Genetics, Functional Genomics, andBreeding” International Journal of Plant Genomics. 2011 (2011); 13pages. In addition, mutations created in other petunia-calibrachoaplants may be used to produce a backcross conversion ofpetunia-calibrachoa that comprises such mutation.

Additional methods include, but are not limited to, expression vectorsintroduced into plant tissues using a direct gene transfer method, suchas microprojectile-mediated delivery, DNA injection, electroporation,and the like. More preferably, expression vectors are introduced intoplant tissues by using either microprojectile-mediated delivery with abiolistic device or by using Agrobacterium-mediated transformation.Transformant plants obtained with the protoplasm of the embodiments areintended to be within the scope of the embodiments.

Gene Editing Using CRISPR

Targeted gene editing can be done using CRISPR/Cas9 technology (Saunders& Joung, Nature Biotechnology, 32, 347-355, 2014). CRISPR is a type ofgenome editing system that stands for Clustered Regularly InterspacedShort Palindromic Repeats. This system and CRISPR-associated (Cas) genesenable organisms, such as select bacteria and archaea, to respond to andeliminate invading genetic material. Ishino, Y., et al. J. Bacteriol.169, 5429-5433 (1987). These repeats were known as early as the 1980s inE. coli, but Barrangou and colleagues demonstrated that S. thermophiluscan acquire resistance against a bacteriophage by integrating a fragmentof a genome of an infectious virus into its CRISPR locus. Barrangou, R.,et al. Science 315, 1709-1712 (2007). Many plants have already beenmodified using the CRISPR system, including Petunia. See for example,Zhang, B. et al., “Exploiting the CRISPR/Cas9 System for Targeted GenomeMutagenesis in Petunia” Science Reports, Vol. 6, February 2016.

Gene editing can also be done using crRNA-guided surveillance systemsfor gene editing. Additional information about crRNA-guided surveillancecomplex systems for gene editing can be found in the followingdocuments, which are incorporated by reference in their entirety: U.S.Application Publication No. 2010/0076057 (Sontheimer et al., Target DNAInterference with crRNA); U.S. Application Publication No. 2014/0179006(Feng, CRISPR-CAS Component Systems, Methods, and Compositions forSequence Manipulation); U.S. Application Publication No. 2014/0294773(Brouns et al., Modified Cascade Ribonucleoproteins and Uses Thereof);Sorek et al., Annu. Rev. Biochem. 82:273-266, 2013; and Wang, S. et al.,Plant Cell Rep (2015) 34: 1473-1476.

Therefore, it is another embodiment to use the CRISPR system onpetunia-calibrachoa variety SAKPXC032 to modify traits and resistancesor tolerances to pests, herbicides, and viruses.

Gene Editing Using TALENs

Transcription activator-like effector nucleases (TALENs) have beensuccessfully used to introduce targeted mutations via repair of doublestranded breaks (DSBs) either through non-homologous end joining (NHEJ),or by homology-directed repair (HDR) and homology-independent repair inthe presence of a donor template. Thus, TALENs are another mechanism fortargeted genome editing using SAKPXC032. The technique is well known inthe art; see for example Malzahn, Aimee et al. “Plant genome editingwith TALEN and CRISPR” Cell & bioscience vol. 7 21. 24 Apr. 2017.

Therefore, it is another embodiment to use the TALENs system onpetunia-calibrachoa variety SAKPXC032 to modify traits and resistancesor tolerances to pests, herbicides, and viruses.

Other Methods of Genome Editing

In addition to CRISPR and TALENs, two other types of engineerednucleases can be used for genome editing: engineered homingendonucleases/meganucleases (EMNs), and zinc finger nucleases (ZFNs).These methods are well known in the art. See for example, Petilino,Joseph F. “Genome editing in plants via designed zinc finger nucleases”In Vitro Cell Dev Biol Plant. 51(1): pp. 1-8 (2015); and Daboussi,Fayza, et al. “Engineering Meganuclease for Precise Plant GenomeModification” in Advances in New Technology for Targeted Modification ofPlant Genomes. Springer Science+Business. pp 21-38 (2015).

Therefore, it is another embodiment to use engineered nucleases onpetunia-calibrachoa variety SAKPXC032 to modify traits and resistancesor tolerances to pests, herbicides, and viruses.

Introduction of a New Trait or Locus into Petunia-Calibrachoa VarietySAKPXC032

Petunia-calibrachoa variety SAKPXC032 represents a new variety intowhich a new locus or trait may be introgressed. Direct transformationand backcrossing represent two important methods that can be used toaccomplish such an introgression. The term backcross conversion andsingle locus conversion are used interchangeably to designate theproduct of a backcrossing program.

Molecular Techniques Using Petunia-Calibrachoa Variety SAKPXC032

The advent of new molecular biological techniques has allowed theisolation and characterization of genetic elements with specificfunctions. Traditional plant breeding has principally been the source ofnew germplasm, however, advances in molecular technologies have allowedbreeders to provide varieties with novel and much wanted commercialattributes. Molecular techniques such as transformation are popular inbreeding ornamental plants and well-known in the art. See Vainstein,“Breeding for Ornamentals: Classical and Molecular Approaches,” KluwerAcademic Publishers (2002).

Breeding with Molecular Markers

Molecular markers can also be used during the breeding process for theselection of qualitative traits. For example, markers closely linked toalleles or markers containing sequences within the actual alleles ofinterest can be used to select plants that contain the alleles ofinterest during a backcrossing breeding program. The markers can also beused to select for the genome of the recurrent parent and against thegenome of the donor parent. Using this procedure can minimize the amountof genome from the donor parent that remains in the selected plants. Itcan also be used to reduce the number of crosses back to the recurrentparent needed in a backcrossing program. The use of molecular markers inthe selection process is often called genetic marker enhanced selection.Molecular markers may also be used to identify and exclude certainsources of germplasm as parental varieties or ancestors of a plant byproviding a means of tracking genetic profiles through crosses.Molecular markers, which includes markers identified through the use oftechniques such as Isozyme Electrophoresis, Restriction Fragment LengthPolymorphisms (RFLPs), Randomly Amplified Polymorphic DNAs (RAPDs),Arbitrarily Primed Polymerase Chain Reaction (AP-PCR), DNA AmplificationFingerprinting (DAF), Sequence Characterized Amplified Regions (SCARs),Amplified Fragment Length Polymorphisms (AFLPs), Simple Sequence Repeats(SSRs), and Single Nucleotide Polymorphisms (SNPs), may be used in plantbreeding methods utilizing petunia-calibrachoa variety SAKPXC032. SeeVainstein, “Breeding for Ornamentals: Classical and MolecularApproaches,” Kluwer Academic Publishers (2002).

One use of molecular markers is Quantitative Trait Loci (QTL) mapping.QTL mapping is the use of markers, which are known to be closely linkedto alleles that have measurable effects on a quantitative trait.Selection in the breeding process is based upon the accumulation ofmarkers linked to the positive effecting alleles and/or the eliminationof the markers linked to the negative effecting alleles from the plant'sgenome. See for example, Fletcher, Richard S., et al., “QTL analysis ofroot morphology, flowering time, and yield reveals trade-offs inresponse to drought in Brassica napus Journal of Experimental Biology.66 (1): 245-256 (2014). QTL markers can also be used during the breedingprocess for the selection of qualitative traits. For example, markersclosely linked to alleles or markers containing sequences within theactual alleles of interest can be used to select plants that contain thealleles of interest during a backcrossing breeding program. The markerscan also be used to select for the genome of the recurrent parent andagainst the genome of the donor parent. Using this procedure canminimize the amount of genome from the donor parent that remains in theselected plants. It can also be used to reduce the number of crossesback to the recurrent parent needed in a backcrossing program. The useof molecular markers in the selection process is often called geneticmarker enhanced selection. Molecular markers may also be used toidentify and exclude certain sources of germplasm as parental varietiesor ancestors of a plant by providing a means of tracking geneticprofiles through crosses.

Production of Double Haploids

The production of double haploids can also be used for the developmentof plants with a homozygous phenotype in the breeding program. Forexample, a petunia-calibrachoa plant for which petunia-calibrachoavariety SAKPXC032 is a parent can be used to produce double haploidplants. Double haploids are produced by the doubling of a set ofchromosomes (1N) from a heterozygous plant to produce a completelyhomozygous individual. This can be advantageous because the processomits the generations of selfing needed to obtain a homozygous plantfrom a heterozygous source. For example, see, Ferrie, Alison M. R., etal., “Review of Doubled Haploidy Methodologies in Ornamental Species”Propagation of Ornamental Plants. 11(2): pp. 63-77 (2011).

Thus, an embodiment is a process for making a substantially homozygouspetunia-calibrachoa variety SAKPXC032 progeny plant by producing orobtaining a seed from the cross of petunia-calibrachoa variety SAKPXC032and another petunia-calibrachoa plant and applying double haploidmethods to the F₁ seed or F₁ plant or to any successive filialgeneration.

In particular, a process of making seed retaining the molecular markerprofile of petunia-calibrachoa variety SAKPXC032 is contemplated, suchprocess comprising obtaining or producing F₁ seed for whichpetunia-calibrachoa variety SAKPXC032 is a parent, inducing doubledhaploids to create progeny without the occurrence of meioticsegregation, obtaining the molecular marker profile ofpetunia-calibrachoa variety SAKPXC032, and selecting progeny that retainthe molecular marker profile of petunia-calibrachoa variety SAKPXC032.

Expression Vectors for Petunia-Calibrachoa Transformation: Marker Genes

Plant transformation involves the construction of an expression vectorwhich will function in plant cells. Such a vector comprises DNAcomprising a gene under control of, or operatively linked to, aregulatory element (for example, a promoter). Expression vectors includeat least one genetic marker operably linked to a regulatory element (forexample, a promoter) that allows transformed cells containing the markerto be either recovered by negative selection, i.e., inhibiting growth ofcells that do not contain the selectable marker gene, or by positiveselection, i.e., screening for the product encoded by the geneticmarker. Many commonly used selectable marker genes for planttransformation are well-known in the transformation arts, and include,for example, genes that code for enzymes that metabolically detoxify aselective chemical agent which may be an antibiotic or an herbicide, orgenes that encode an altered target which is insensitive to theinhibitor. A few positive selection methods are also known in the art.

One commonly used selectable marker gene for plant transformation is theneomycin phosphotransferase II (nptII) gene which, when under thecontrol of plant regulatory signals, confers resistance to kanamycin.Another commonly used selectable marker gene is the hygromycinphosphotransferase gene which confers resistance to the antibiotichygromycin.

Selectable marker genes for plant transformation not of bacterial origininclude, for example, mouse dihydrofolate reductase, plant5-enolpyruvylshikimate-3-phosphate synthase, and plant acetolactatesynthase (Eichholtz, et al., Somatic Cell Mol. Genet., 13:67 (1987);Shah, et al., Science, 233:478 (1986); Charest, et al., Plant Cell Rep.,8:643 (1990)).

Another class of marker genes for plant transformation requiresscreening of presumptively transformed plant cells, rather than directgenetic selection of transformed cells, for resistance to a toxicsubstance such as an antibiotic. These genes are particularly useful toquantify or visualize the spatial pattern of expression of a gene inspecific tissues and are frequently referred to as reporter genesbecause they can be fused to a gene or gene regulatory sequence for theinvestigation of gene expression. Commonly used marker genes forscreening presumptively transformed cells include β-glucuronidase (GUS),β-galactosidase, luciferase, and chloramphenicol acetyltransferase(Jefferson, R. A., Plant Mol. Biol. Rep., 5:387 (1987); Teeri, et al.,EMBO J., 8:343 (1989); Koncz, et al., Proc. Natl. Acad. Sci. USA, 84:131(1987); DeBlock, et al., EMBO J., 3:1681 (1984)).

Expression Vectors for Petunia-Calibrachoa Transformation: Promoters

Genes included in expression vectors must be driven by a nucleotidesequence comprising a regulatory element (for example, a promoter).Several types of promoters are well known in the transformation arts asare other regulatory elements that can be used alone or in combinationwith promoters.

As used herein, “promoter” includes reference to a region of DNAupstream from the start of transcription and involved in recognition andbinding of RNA polymerase and other proteins to initiate transcription.A “plant promoter” is a promoter capable of initiating transcription inplant cells. Examples of promoters under developmental control includepromoters that preferentially initiate transcription in certain tissues,such as leaves, roots, seeds, fibers, xylem vessels, tracheids, orsclerenchyma. Such promoters are referred to as “tissue-preferred.”Promoters that initiate transcription only in a certain tissue arereferred to as “tissue-specific.” A “cell-type” specific promoterprimarily drives expression in certain cell types in one or more organs,for example, vascular cells in roots or leaves. An “inducible” promoteris a promoter which is under environmental control. Examples ofenvironmental conditions that may affect transcription by induciblepromoters include anaerobic conditions or the presence of light.Tissue-specific, tissue-preferred, cell-type specific, and induciblepromoters constitute the class of “non-constitutive” promoters. A“constitutive” promoter is a promoter that is active under mostenvironmental conditions. Many types of promoters are well known in theart.

Signal Sequences for Targeting Proteins to Subcellular Compartments

Transport of a protein produced by transgenes to a subcellularcompartment, such as the chloroplast, vacuole, peroxisome, glyoxysome,cell wall, or mitochondrion, or for secretion into the apoplast, isaccomplished by means of operably linking the nucleotide sequenceencoding a signal sequence to the 5′ and/or 3′ region of a gene encodingthe protein of interest. Targeting sequences at the 5′ and/or 3′ end ofthe structural gene may determine during protein synthesis andprocessing where the encoded protein is ultimately compartmentalized.Many signal sequences are well-known in the art. See, for example,Becker, et al., Plant Mol. Biol., 20:49 (1992); Knox, C., et al., PlantMol. Biol., 9:3-17 (1987); Lerner, et al., Plant Physiol., 91:124-129(1989); Frontes, et al., Plant Cell, 3:483-496 (1991); Matsuoka, et al.,Proc. Natl. Acad. Sci., 88:834 (1991); Gould, et al., J. Cell. Biol.,108:1657 (1989); Creissen, et al., Plant 2:129 (1991); Kalderon, et al.,Cell, 39:499-509 (1984); Steifel, et al., Plant Cell, 2:785-793 (1990).

Foreign Protein Genes: Transformation

Various promoters, targeting sequences, enhancing sequences, and otherDNA sequences can be inserted into the genome for the purpose ofaltering the expression of genes.

Many techniques for altering gene expression are well-known to one ofskill in the art, including, but not limited to, knock-outs (such as byinsertion of a transposable element such as Mu (Vicki Chandler, TheMaize Handbook, Ch. 118 (Springer-Verlag 1994)) or other geneticelements such as a FRT, Lox, or other site specific integration sites;antisense technology (see, e.g., Sheehy, et al., PNAS USA, 85:8805-8809(1988) and U.S. Pat. Nos. 5,107,065, 5,453,566, and 5,759,829);co-suppression (e.g., Taylor, Plant Cell, 9:1245 (1997); Jorgensen,Trends Biotech., 8(12):340-344 (1990); Flavell, PNAS USA, 91:3490-3496(1994); Finnegan, et al., Bio/Technology, 12:883-888 (1994); Neuhuber,et al., Mol. Gen. Genet., 244:230-241 (1994)); RNA interference (Napoli,et al., Plant Cell, 2:279-289 (1990); U.S. Pat. No. 5,034,323; Sharp,Genes Dev., 13:139-141 (1999); Zamore, et al., Cell, 101:25-33 (2000);Montgomery, et al., PNAS USA, 95:15502-15507 (1998)), virus-induced genesilencing (Burton, et al., Plant Cell, 12:691-705 (2000); Baulcombe,Curr. Op. Plant Bio., 2:109-113 (1999)); target-RNA-specific ribozymes(Haseloff, et al., Nature, 334:585-591 (1988)); hairpin structures(Smith, et al., Nature, 407:319-320 (2000); U.S. Pat. Nos. 6,423,885,7,138,565, 6,753,139, and 7,713,715); MicroRNA (Aukerman & Sakai, PlantCell, 15:2730-2741 (2003)); ribozymes (Steinecke, et al., EMBO J.,11:1525 (1992); Perriman, et al., Antisense Res. Dev., 3:253 (1993));oligonucleotide mediated targeted modification (e.g., U.S. Pat. Nos.6,528,700 and 6,911,575); Zn-finger targeted molecules (e.g., U.S. Pat.Nos. 7,151,201, 6,453,242, 6,785,613, 7,177,766 and 7,788,044);transposable elements (e.g. Dubin, M. J., et al., Transposons: ablessing curse, Current opinion in plant biology, Vol: 42, Page: 23-29,2018 and Eric T. Johnson, Jesse B. Owens & Stefan Moisyadi (2016) Vastpotential for using the piggyBac transposon to engineer transgenicplants at specific genomic locations, Bioengineered, 7:1, 3-6) and othermethods or combinations of the above methods known to those of skill inthe art.

The foregoing methods for transformation may be used for producing atransgenic variety. The transgenic variety could then be crossed withanother (non-transformed or transformed) variety in order to produce anew transgenic variety. Alternatively, a genetic trait that has beenengineered into a particular petunia-calibrachoa variety using theforegoing transformation techniques could be moved into another varietyusing traditional backcrossing techniques that are well known in theplant breeding arts. For example, a backcrossing approach could be usedto move an engineered trait from a public, non-elite variety into anelite variety, or from a variety containing a foreign gene in its genomeinto a variety or varieties that do not contain that gene. As usedherein, “crossing” can refer to a simple x by y cross or the process ofbackcrossing depending on the context.

Likewise, by means of one embodiment, genes can be expressed intransformed plants. More particularly, plants can be geneticallyengineered to express various phenotypes of interest, including, but notlimited to, genes that confer resistance to pests or disease, genes thatconfer resistance to an herbicide, genes that confer or contribute to avalue-added or desired trait, genes that control male sterility, genesthat create a site for site specific DNA integration, and genes thataffect abiotic stress resistance. Many hundreds if not thousands ofdifferent genes are known and could potentially be introduced into aplant according to the invention. Non-limiting examples of particulargenes and corresponding phenotypes one may choose to introduce into aplant include one or more genes for insect tolerance, such as a Bacillusthuringiensis (Bt.) gene, pest tolerance such as genes for fungaldisease control, herbicide tolerance such as genes conferring glyphosatetolerance, and genes for quality improvements such as, environmental orstress tolerances, or any desirable changes in plant physiology, growth,development, morphology or plant product(s). For example, structuralgenes would include any gene that confers insect tolerance including butnot limited to a Bacillus insect control protein gene as described in WO99/31248, herein incorporated by reference in its entirety, U.S. Pat.No. 5,689,052, herein incorporated by reference in its entirety, U.S.Pat. Nos. 5,500,365 and 5,880,275, herein incorporated by reference intheir entirety. In another embodiment, the structural gene can confertolerance to the herbicide glyphosate as conferred by genes including,but not limited to Agrobacterium strain CP4 glyphosate resistant EPSPSgene (aroA:CP4) as described in U.S. Pat. No. 5,633,435, hereinincorporated by reference in its entirety, or glyphosate oxidoreductasegene (GOX) as described in U.S. Pat. No. 5,463,175, herein incorporatedby reference in its entirety. Alternatively, the DNA coding sequencescan affect these phenotypes by encoding a non-translatable RNA moleculethat causes the targeted inhibition of expression of an endogenous gene,for example via antisense- or cosuppression-mediated mechanisms (see,for example, Bird et al., Biotech. Gen. Engin. Rev., 9:207, 1991). TheRNA could also be a catalytic RNA molecule (i.e., a ribozyme) engineeredto cleave a desired endogenous mRNA product (see for example, Gibson andShillito, Mol. Biotech., 7:125, 1997). Thus, any gene which produces aprotein or mRNA which expresses a phenotype or morphology change ofinterest is useful for the practice of one or more embodiments.

Tissue Culture

Further reproduction of the variety can occur by tissue culture andregeneration. Tissue culture of various tissues of ornamental plants andpetunia-calibrachoa SAKPXC032 and regeneration of plants therefrom iswell-known and widely published. For example, reference may be had toValla Rego, Luciana et al., Crop Breeding and Applied Technology. 1(3):283-300 (2001); Komatsuda, T., et al., Crop Sci., 31:333-337 (1991);Stephens, P. A., et al., Theor. Appl. Genet., 82:633-635 (1991);Komatsuda, T., et al., Plant Cell, Tissue and Organ Culture, 28:103-113(1992); Dhir, S., et al., Plant Cell Reports, 11:285-289 (1992); Pandey,P., et al., Japan J. Breed., 42:1-5 (1992); and Shetty, K., et al.,Plant Science, 81:245-251 (1992). Thus, another embodiment is to providecells which upon growth and differentiation produce petunia-calibrachoaplants having the physiological and morphological characteristics ofpetunia-calibrachoa SAKPXC032 described in the present application.

Regeneration refers to the development of a plant from tissue culture.The term “tissue culture” indicates a composition comprising isolatedcells of the same or a different type or a collection of such cellsorganized into parts of a plant. Exemplary types of tissue cultures areprotoplasts, calli, plant clumps, and plant cells that can generatetissue culture that are intact in plants or parts of plants, such asembryos, pollen, flowers, seeds, pods, petioles, leaves, stems, roots,root tips, anthers, pistils, and the like. Means for preparing andmaintaining plant tissue culture are well known in the art. By way ofexample, a tissue culture comprising organs has been used to produceregenerated plants. U.S. Pat. Nos. 5,959,185, 5,973,234, and 5,977,445describe certain techniques, the disclosures of which are incorporatedherein by reference.

While a number of exemplary aspects and embodiments have been discussedabove, those of skill in the art will recognize certain modifications,permutations, additions and sub-combinations thereof. It is thereforeintended that the following appended claims and claims hereafterintroduced are interpreted to include all such modifications,permutations, additions, and sub-combinations as are within their truespirit and scope.

One or more aspects may be embodied in other specific forms withoutdeparting from its spirit or essential characteristics. The describedembodiments are to be considered in all respects only as illustrativeand not restrictive. The scope of the embodiments is, therefore,indicated by the appended claims rather than by the foregoingdescription. All changes which come within the meaning and range ofequivalency of the claims are to be embraced within their scope. Theforegoing discussion of the embodiments has been presented for purposesof illustration and description. The foregoing is not intended to limitthe embodiments to the form or forms disclosed herein. In the foregoingDetailed Description for example, various features of the embodimentsare grouped together in one or more embodiments for the purpose ofstreamlining the disclosure. This method of disclosure is not to beinterpreted as reflecting an intention that the claimed embodimentsrequire more features than are expressly recited in each claim. Rather,as the following claims reflect, inventive aspects lie in less than allfeatures of a single foregoing disclosed embodiment. Thus, the followingclaims are hereby incorporated into this Detailed Description, with eachclaim standing on its own as a separate preferred embodiment.

Moreover, though the description of the embodiments has includeddescription of one or more embodiments and certain variations andmodifications, other variations and modifications are within the scopeof the embodiments (e.g., as may be within the skill and knowledge ofthose in the art, after understanding the present disclosure). It isintended to obtain rights which include alternative embodiments to theextent permitted, including alternate, interchangeable and/or equivalentstructures, functions, ranges or acts to those claimed, whether or notsuch alternate, interchangeable and/or equivalent structures, functions,ranges or acts are disclosed herein, and without intending to publiclydedicate any patentable subject matter.

The terms “comprising,” “having,” “including,” and “containing” are tobe construed as open-ended terms (i.e., meaning “including, but notlimited to,”) unless otherwise noted. Recitation of ranges of valuesherein are merely intended to serve as a shorthand method of referringindividually to each separate value falling within the range, unlessotherwise indicated herein, and each separate value is incorporated intothe specification as if it were individually recited herein. Forexample, if the range 10-15 is disclosed, then 11, 12, 13, and 14 arealso disclosed. All methods described herein can be performed in anysuitable order unless otherwise indicated herein or otherwise clearlycontradicted by context. The use of any and all examples, or exemplarylanguage (e.g., “such as”) provided herein, is intended merely to betterilluminate the embodiments and does not pose a limitation on the scopeof the embodiments unless otherwise claimed. No language in thespecification should be construed as indicating any non-claimed elementas essential to the practice of one or more embodiments.

DEPOSIT INFORMATION

A plant tissue deposit of the Sakata Seed Corporation proprietarypetunia-calibrachoa variety SAKPXC032 disclosed above and recited in theappended claims is maintained by Sakata Seed Corporation. A deposit willbe made with the Provasoli-Guillard National Center for Marine Algae andMicrobiota, Bigelow Laboratory for Ocean Sciences, 60 Bigelow Drive,East Boothbay, Me. 04544, United States. Access to this deposit will beavailable during the pendency of this application to persons determinedby the Commissioner of Patents and Trademarks to be entitled theretounder 37 C.F.R. 1.14 and 35 U.S.C. § 122. Upon allowance of any claimsin this application, all restrictions on the availability to the publicof the variety will be irrevocably removed by affording access to adeposit of the plant tissue deposit of the same variety with theProvasoli-Guillard National Center for Marine Algae and Microbiota,Bigelow Laboratory for Ocean Sciences. The deposit will be maintained inthe depository for a period of 30 years, or 5 years after the lastrequest, or for the effective life of the patent, whichever is longer,and will be replaced if necessary, during that period.

What is claimed is:
 1. A plant of petunia-calibrachoa variety SAKPXC032,wherein a representative sample of plant tissue of SAKPXC032 wasdeposited under NCMA No. ______.
 2. A plant, or a plant part thereofproduced by growing the plant of claim 1, wherein the plant or plantpart comprises at least one cell of petunia-calibrachoa varietySAKPXC032.
 3. A petunia-calibrachoa plant, or part thereof, having allof the physiological and morphological characteristics of thepetunia-calibrachoa plant of claim
 1. 4. A tissue or cell culture ofregenerable cells produced from the plant of claim
 1. 5. The tissue orcell culture of claim 4, comprising tissues or cells from a plant partselected from the group consisting of leaves, pollen, embryos,cotyledons, hypocotyl, meristematic cells, roots, root tips, pistils,anthers, flowers, and stems.
 6. A petunia-calibrachoa plant regeneratedfrom the tissue or cell culture of claim 5, wherein said plant has allof the morphological and physiological characteristics ofpetunia-calibrachoa SAKPXC032 listed in Table
 1. 7. A method ofvegetatively propagating the plant of claim 1, comprising the steps of:collecting tissue or cells capable of being propagated from said plant;cultivating said tissue or cells to obtain proliferated shoots; androoting said proliferated shoots to obtain rooted plantlets; orcultivating said tissue or cells to obtain proliferated shoots, or toobtain plantlets.
 8. A petunia-calibrachoa plant produced by growing theplantlets or proliferated shoots of claim
 7. 9. A method for producingan embryo or seed, wherein the method comprises crossing the plant ofclaim 1 with another plant and harvesting the resultant embryo or seed.10. A method of determining the genotype of the petunia-calibrachoaplant of claim 1, wherein said method comprises obtaining a sample ofnucleic acids from said plant and detecting in said nucleic acids aplurality of polymorphisms.
 11. A method of producing apetunia-calibrachoa plant resistant to the group consisting ofherbicides, insecticides, and disease, wherein the method comprisestransforming the petunia-calibrachoa plant of claim 1 with a transgene,and wherein said transgene confers resistance to an herbicide,insecticide, or disease.
 12. An herbicide, insecticide, or diseaseresistant plant produced by the method of claim
 11. 13. A method fordeveloping a petunia-calibrachoa plant in a plant breeding program,comprising applying plant breeding techniques comprising crossing,recurrent selection, mutation breeding, wherein said mutation breedingselects for a mutation that is spontaneous or artificially induced,backcrossing, pedigree breeding, marker enhanced selection,haploid/double haploid production, or transformation to a plant ofpetunia-calibrachoa variety SAKPXC032, wherein a representative sampleof plant tissue of SAKPXC032 was deposited under NCMA No. ______, or itsparts, wherein application of said techniques results in development ofa petunia-calibrachoa plant.
 14. A method of introducing a mutation intothe genome of petunia-calibrachoa plant SAKPXC032, said methodcomprising mutagenesis of the plant, or plant part thereof, of claim 1,wherein said mutagenesis is selected from the group consisting oftemperature, long-term seed storage, tissue culture conditions, ionizingradiation, chemical mutagens, or targeting induced local lesions ingenomes, and wherein the resulting plant comprises at least one genomemutation.
 15. A method of editing the genome of petunia-calibrachoaplant SAKPXC032, said method comprising editing the genome of the plant,or plant part thereof, wherein a representative sample of plant tissueof SAKPXC032 was deposited under NCMA No. ______, wherein said method isselected from the group comprising zinc finger nucleases, transcriptionactivator-like effector nucleases (TALENs), engineered homingendonucleases/meganucleases, and the clustered regularly interspacedshort palindromic repeat (CRISPR)-associated protein9 (Cas9) system. 16.A petunia-calibrachoa plant produced by the method of claim
 15. 17. Apetunia-calibrachoa seed produced by growing the plant of claim
 1. 18. Amethod of producing a petunia-calibrachoa plant, or part thereof,produced by growing the seed of claim
 17. 19. The method of claim 9,further comprising producing a plant, or a part thereof, from theresultant embryo or seed.